510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K960621Substantially Equivalent

Expandacell Instrument Wipe

Summit Medical, LLC, Englewood CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K960621 is the FDA 510(k) clearance record for EXPANDACELL INSTRUMENT WIPE, a class I device, cleared for Shippert Medical Technologies Corp. on under FDA product code GEC (Brush, Scrub, Operating-Room). FDA records list 27 510(k) clearances for SUMMIT MEDICAL LLC, from to . As of , FDA records show no recalls naming K960621.

Clearance record

Decision date
Received
(48 days to decision)
Product code
GEC Brush, Scrub, Operating-Room
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Shippert Medical Technologies Corp. 7002 S. Revere Pkwy., Englewood CO
510(k) summary
Summary
Third party review
No

Clearances, product code GEC

Trailing 12 months

FDA records hold no clearances under product code GEC in the trailing twelve months.

FDA records show no clearances under product code GEC in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GEC, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260